A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv934169



Internal ID16228125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240923534..240924859hg38UCSC Ensembl
Innerchr2:241862951..241864276hg19UCSC Ensembl
Innerchr2:241511624..241512949hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381326
hg191326
hg181326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584898
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv934169
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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